Home NDC 11822-5768-6 Oral Antivavity
Product NDC 11822-5768
Requested package NDC 11822-5768-6
11-digit product format 118225768
Labeler code 11822
Product ID 11822-5768_1859d114-a81f-4b61-8f0a-4a04de4d9135
Type HUMAN OTC DRUG
Nonproprietary name Sodium fluoride
Dosage form MOUTHWASH
Route ORAL
Labeler Rite Aid
Application part355
Marketing category OTC MONOGRAPH FINAL
Marketing start 2022-12-05
Marketing end 0000-00-00
Substance SODIUM FLUORIDE
Active strength 0 mg/mL
NDC exclude flag No
Listing certified through 2023-12-31
Current FDA listing Historical FDA.report record Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 excluded package package 11822-5768 11822-5768-6 D Discontinued by firm excluded / ndc_excluded.zip d630ba8d3edf…732f749b63fb…
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 11822-5768 ORAL ANTIVAVITY (SODIUM FLUORIDE) MOUTHWASH [RITE AID] 2 Legacy NDC 20240926_903c2363-9d4c-4f9c-8865-514c1ea4ce72.zip
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 11822-5768-6 11822576806 1000 mL in 1 BOTTLE (11822-5768-6) 1000 ml 2022-12-05 0000-00-00 No No Current